A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16265476



Internal ID20474694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:49997245..49998046hg38UCSC Ensembl
chr14:50463963..50464764hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg38802
hg19802
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4755327
Supporting Variants
Samples
Known GenesC14orf182
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16265476
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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